Expert advice on how to write and edit scientific and medical texts, technical documents and those documents needed for regulatory submission
11 Feb 2020
Also on: 25 Sep 2020
Book by 20 Dec to save
£100 / €140 / $156
This course will take participants through all of the necessary steps to obtain marketing authorisation for a feed additive in the European Union.
We can customise this course to meet your requirements.
Success in the pharmaceutical industry depends on the speed and efficiency of new drug approvals and the quality of documentation submitted to the regulatory authorities. This intensive practical medical writing course will benefit participants by enabling them to achieve this standard.
14-16 Oct 2019
Also on: 18 May 2020
Presentations will cover the regulatory framework, pharmaceutical, toxicological and pharmacological data, safety risk assessments, pre-clinical and clinical data, Detailed and Critical Summaries and regulatory submissions
26-27 Nov 2019
Also on: 24 Mar 2020
This practical four day course provides a comprehensive understanding of a veterinary medicine development in the EU and USA.